The purpose of this study is to evaluate the safety and efficacy of HepaSphere interventional therapy using digital subtraction Angiography(DSA)for pancreatic cancer.
By enrolling patients with pancreatic cancer adapted to enrolled criteria, this study will document for the first time the safety and the short and long term efficacy of HepaSphere interventional therapy using digital subtraction Angiography(DSA)for pancreatic cancer.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
pancreatic cancer patients received HepaSphere interventional therapy using the digital subtraction angiography(DSA)
Central laboratory in Fuda cancer hospital
Guangzhou, Guangdong, China
Number of participants with Adverse events
Time frame: 1 year
Percentage of lesions that show no sign of recurrence 12 months after interventional therapy
Time frame: 1 year
Progress free disease (PFS)
Time frame: 1 year
Overall survival (OS)
Time frame: 3 year
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